Blood & Tissue

Visualizing a new data-centered quality paradigm. When the first Nokia and Motorola cell phones that were affordable and small enough to fit in your pocket hit the market...

Automation can help pharmaceutical and biologics companies along the path to a global product launch. This white paper identifies common problems with submissions and how best to address them.

This white paper explores the range of software solutions targeting organizations in the blood and biologics industry, from EDMS to QMS. Evaluate and select the most suitable solution for them.

This Q&A breaks down the key requirements of 21 CFR Part 1270 (Human Tissue Intended for Transplantation) and Part 1271 (Human Cells, Tissues, and Cellular Tissue-Based Products).

MasterControl Registrations for eCTD is a cloud-based solution designed to streamline content generation and the collection and management of artifacts required for regulatory submission.

Learn about the most common 483 observations and audit findings, and avoid warning letters by staying compliant and addressing issues in the stipulated time period.